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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Dietary Supplements

Hard Steel Capsules and Liquid Recalled for Undeclared Drug Ingredients

Agency Publication Date: October 2, 2024
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Summary

Supercore Products Group Inc. is recalling Hard Steel Capsules and Gold Hard Steel Plus Liquid because they were marketed without FDA approval and contain undeclared acetaminophen and sildenafil (the active ingredient in Viagra). The recall affects approximately 1,344 units, including 729 boxes of capsules and 615 bottles of the liquid product. These items were distributed nationwide in the United States and several other countries.

Risk

Undeclared sildenafil can interact with nitrates found in some prescription drugs (such as nitroglycerin), which may lower blood pressure to dangerous or life-threatening levels. Additionally, undeclared acetaminophen poses a serious risk of liver damage if the user is already taking other medications containing acetaminophen.

What You Should Do

  1. This recall affects all lots of Hard Steel Capsules (sold in boxes of 10, 20, or 30) and Gold Hard Steel Plus Liquid (2 FL OZ bottles with UPC 787188873199).
  2. If you have health concerns, contact your healthcare provider or pharmacist.
  3. Return any unused product to the place of purchase for a refund, throw it away, or contact Supercore Products Group Inc. for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Hard Steel Capsules
Variants: 1 count blister packs, Boxes of 10, Boxes of 20, Boxes of 30
Lot Numbers:
All lots

Manufactured in U.S.A.

Product: Gold Hard Steel Plus Liquid (2 FL OZ)
Variants: 2 FL OZ bottles
UPC Codes:
787188873199
Lot Numbers:
All lots

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94949
Status: Active
Manufacturer: Supercore Products Group Inc.
Manufactured In: United States
Units Affected: 2 products (729; 615)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท FDA Press Release ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.